2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine

    • Product Name: 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine
    • Chemical Name (IUPAC): 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine
    • CAS No.: 104241-86-3
    • Chemical Formula: C9H12ClNO
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    103460

    Iupac Name 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine
    Molecular Formula C9H12ClNO
    Molecular Weight 185.65 g/mol
    Cas Number 343268-60-4
    Appearance Colorless to pale yellow liquid
    Boiling Point Undetermined; estimated around 255°C
    Density Approx. 1.13 g/cm3 (estimated)
    Solubility In Water Low solubility
    Smiles CC1=NC(=C(C(=C1OC)C)CCl)C
    Inchi InChI=1S/C9H12ClNO/c1-6-4-8(3)11-5-9(6)13-7(2)10/h4-5H,1-3H3
    Flash Point Estimated 107°C
    Synonyms 2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine
    Storage Conditions Store in a cool, dry, well-ventilated place

    As an accredited 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, sealed with a Teflon-lined cap, labeled "2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine, 25g, For laboratory use only."
    Container Loading (20′ FCL) 20′ FCL can load 10–12 MT of 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine in steel drums/palletized for export.
    Shipping 2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine ships in a sealed, chemical-resistant container, labeled according to GHS/OSHA standards. It is transported as a hazardous material, typically under 25°C, avoiding direct sunlight, heat, and moisture. Appropriate documentation and handling precautions are provided to ensure safe delivery compliant with applicable regulations.
    Storage 2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, ignition sources, and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Use proper chemical storage cabinets and ensure clear labeling to avoid accidental misuse. Handle with appropriate protective equipment.
    Shelf Life 2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine typically has a shelf life of 2 years when stored in a cool, dry place.
    Application of 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine

    Purity 98%: 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal byproduct formation.

    Molecular weight 185.67 g/mol: 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine of molecular weight 185.67 g/mol is used in agrochemical research, where consistent formulation and reproducible results are achieved.

    Melting point 42–45°C: 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine with a melting point of 42–45°C is used in solid compound screening, where uniform melting behavior facilitates automated processing.

    Stability temperature up to 80°C: 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine stable up to 80°C is used in thermal reaction protocols, where it maintains compound integrity during scale-up operations.

    Particle size <50 μm: 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine with particle size below 50 μm is used in homogeneous mixing for fine chemical blending, where it promotes rapid dissolution and uniform distribution.

    Water content <0.5%: 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine with water content less than 0.5% is used in moisture-sensitive catalysis, where it prevents hydrolysis and preserves reagent potency.

    Residual solvent <200 ppm: 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine with residual solvent below 200 ppm is used in active pharmaceutical ingredient (API) manufacturing, where compliance with regulatory purity standards is maintained.

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    Certification & Compliance
    More Introduction

    Introducing 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine: Product Insights from the Manufacturer

    At our facility, we have spent years perfecting the production techniques behind high-value intermediates like 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine. Few compounds in the pyridine family have had such a transformative role for the pharmaceutical and agrochemical sectors. A simple look at its structure—anchored by its distinctive chloro and methoxy substitutions—shows why many research teams keep it on their shortlist for building specialized pyridine frameworks. The choice to commercialize this particular derivative was not random. Before including it in our line, we observed a growing demand for core structures capable of streamlined downstream functionalization, especially through its chloromethyl group. Years of pilot projects and close collaboration with process chemists shaped our current approach.

    Model and Purity Expectations

    We produce 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine to meet tight purity standards essential for reliable reactions further down the line. Most clients request material >98% pure on GC, so all shipments meet or exceed that threshold. Routine batches yield a crystalline, pale yellow to off-white solid, which remains stable under standard warehouse conditions when kept away from moisture. While some expect only lab-scale reliability, we have scaled batches upward without sacrificing isomeric precision or consistency. Our synthetic pathway gives us a high level of control over contaminant profiles; side products fall below the strictest limits demanded in regulated environments.

    Applications Driven by Structure

    This compound is more than a generic building block. Over the years, our technical support team has answered dozens of requests about the reactivity of its chloromethyl handle. Many chemists value it for direct nucleophilic substitution, making it practical for producing subsequent pyridine-based linkers, herbicide intermediates, and certain pharmaceutical cores—especially in cases where other available chloromethyl pyridines proved too reactive or lacking in selectivity. The O-methoxy group at the 4-position not only nudges electron density in subtle but important directions, but also opens alternative synthetic routes unavailable with simpler pyridine analogs. The two methyl groups at positions 3 and 5 create a steric environment that affects both reactivity and final product stability. In practical terms, we see this reflected in several clients’ ability to achieve higher yields or avoid unwanted side reactions by switching to this exact structure from more basic pyridine compounds.

    Why Formulation and Handling Matter

    Having produced hundreds of kilograms at a time, we've learned a few lessons about this compound’s quirks. For instance, its solid form makes weighing and dosing more straightforward, but the chloromethyl group remains sensitive to hydrolysis if left exposed to high humidity. To ensure consistent downstream work, we tightly seal all containers with robust liners and limit atmospheric access. Feedback from our synthesis partners led us to reinforce container seals after one too many cases of performance drop-offs in older competitor samples. We recommend neutral inert atmospheres for long-term storage, a practice adopted by leading process teams in Europe and North America. There are no solvated grades—only pure, isolated compound direct from the last stage of our proprietary process—because we saw mix-and-match solvent lots lead to unpredictable results in key transformations. As a rule, we keep moisture and handling controls tight all the way through filling, packaging, and transport. This level of discipline rarely gets mentioned in catalogs, but process outcomes depend on it.

    Comparisons: Standing Apart from Other Pyridine Derivatives

    Many manufacturers offer pyridine intermediates with simple substituents, but this particular molecule remains a step above in terms of tunable reactivity. The combined presence of chloromethyl, methoxy, and methyl groups means it won’t behave like unsubstituted 2-chloromethylpyridine or 2-chloromethyl-4-methylpyridine. The nuance comes out in competitive reactions—clients regularly tell us that undesired alkylations or byproduct formation drop substantially with our version, especially under mild conditions. The methoxy group reduces uncontrolled polymerizations or resin formation, a point proven by process chemists scaling up complex coupling reactions. When clients previously used unsubstituted analogs, they often fought unwanted chlorination or slow conversion. With ours, the presence of both electron-donating and electron-withdrawing groups gives better balance and selectivity. The two methyl groups help lock in regioselectivity and dictate which positions on the ring remain open for further transformation. A direct side-by-side run with alternative pyridine derivatives almost always convinces skeptical chemists of this molecule's distinct reactivity benefits.

    Supporting a Range of End Uses

    The dominant portion of orders comes from pharmaceutical process development groups. They favor this compound for its ability to create potent azine cores, which in turn form the basis for various active ingredients. On the agrochemical front, a few specific insecticide and herbicide candidates rely on the precise substitution pattern offered here, especially in combinatorial trials requiring stepwise functionalization. The chloromethyl group allows for simple conversion into a variety of quaternary ammonium salts or for simple displacement with amines, thiols, and alkoxides. Lab notebooks on our own benches often show this sequence used to create libraries of sulfonamides, carbamates, and new heterocyclic systems that have applications well beyond drug research. While we hesitate to make blanket claims, our records suggest this structure outperforms several traditional building blocks for those targeting robust drug-like scaffolds. We have received feedback reflecting a measurable improvement in synthetic throughput, especially where difficult couplings or multi-component reactions are involved.

    From Lab Scale to Bulk Production

    Our journey as direct producers has covered the spectrum from grams for R&D work to multi-ton supplies needed for late-stage clinical supply chains. We remember the transition from glassware to jacketed reactors—a point that brought new challenges in reaction exotherms, heat transfer, and micro-scale precipitate formation. Over the years, we installed isolation and drying equipment dedicated to this product because it responds best to careful handling at every stage. Other facilities, cutting corners, have shipped material with unknown amounts of early-stage contaminants; our batch tracking and analytical controls catch those before release. Scaling up required us to refine not just reactor designs but also our upstream reagent purification and downstream crystallization. That diligence shows in product reproducibility, something repeated clients reference as a deciding factor in their sourcing decisions. Laboratory personnel regularly comment on how few purity fluctuations they observe between lots, a direct outcome of our attention to detail. The lesson was clear early on: consistent reaction conditions and process feedback loops guarantee downstream success for everyone relying on our supply.

    Safety and Regulatory Benchmarks

    Decades of direct handling taught us to respect both product potency and regulatory compliance. 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine features a highly reactive chloromethyl group, making proper protective measures essential in all handling scenarios. Every handler in our facility uses full PPE and containment hoods—something learned after early-phase process reviews flagged airborne trace exposure as a meaningful risk. We maintain records and coordinate with safety authorities every year to keep hazard communications, labeling, and disposal procedures up-to-date with current standards. For pharma and crop protection companies with global ties, we commit to full traceability. Transparency about production methods and impurity profiles aligns with quality-assurance needs across regulated industries. By keeping batch certifications in strict order, we help every user document the provenance and stability of every shipment—a key factor as cross-border regulations tighten. We never compromise here; keeping end users safe demands material free of high-risk residues or unexpected lot mislabeling. All feedback loops between our QA teams and outside auditors are direct and corrective, fostering a culture where problems get solved—not swept aside.

    Cost and Practicality in the Real World

    Many assume that specialty intermediates carry a price premium for laboratory-scale reliability, but our large-volume clients have helped anchor efficiencies that bring per-kilogram costs in line with bulk commodity standards. We found that automating filtration, drying, and packaging steps provided real cost improvement, making this compound accessible for both niche R&D and high-throughput manufacturing teams. Bulk contracts permitted us to optimize procurement of key reagents, reducing downstream price spikes during volatile years. By tracking market demand and avoiding excess inventory buildup, we avoid costly warehouse aging, which in turn reduces the risk of off-spec shipments from outdated stock. Over-production runs or stockpiling rarely pays off in this segment; tight inventory control keeps costs in check and assures every lot is as fresh and reactive as possible at delivery. Smaller clients sometimes worry about custom batch minimums; our experience supports creative approaches to splitting lots and scheduling campaigns in ways that balance low-MOQ flexibility with realistic production economics.

    The Human Element: Experienced Insight

    We build relationships with R&D and process chemists, not anonymous buyers. Phone calls and lab visits revealed that tiny missteps—mislabeled lot numbers, minor solvent impurities, or ambiguous COAs—can derail whole project timetables. As the direct manufacturer, we've been invited dozens of times to diagnose stalled reactions or unexplained side product formation. Once, a long-time client sent us an urgent overnight sample; our in-house team ran detailed analytical work and traced the issue to a supplier's subpar batch that entered their workflow. After identifying the contaminant, we overhauled not only their process but also enhanced our internal QC to catch similar risks before they leave our gates. The lesson reinforced the value of direct lines of communication—a benefit only manufacturers can offer. There is no substitute for firsthand technical knowledge combined with intimate process familiarity. Each inbound request, whether a query about reactivity or a concern about regulatory documentation, gets routed to scientists who have direct production and R&D experience—not generic customer service scripts. Our experience grows with every unique application and every problem solved alongside our clients.

    A Closer Look at Competitor Offerings

    Some labs receive 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine from brokers or re-packagers along circuitous global supply chains. In our view, each extra handling step adds risk—risk of contamination, unintended blending, or regulatory oversight errors. By controlling the entire supply chain from raw materials to final packaging, we guarantee that our variant is exactly as described. Few competitors offer full batch traceability and real-time operational data from synthesis through final dispatch; we do. A few outside sources have sent out product released to spec on only one or two analytical markers. We verify by multi-method analysis—GC, NMR, and occasionally LC-MS—to confirm both structure and purity. Over the years, we have seen third-party samples arrive with incorrect or ambiguous substitution patterns. Every time, a direct comparison with our spectrum resolved disputes, and process teams got their chemistry back on track. Direct manufacturing oversight matters, and repeat projects with multinational clients have proven the value of this higher standard.

    Sustainability: Greener Chemistry on the Factory Floor

    As chemistry moves forward, we have worked to align production of this intermediate with modern green chemistry principles. Beginning with solvent recovery, we invested in closed-loop recycling systems, reducing both input costs and environmental impact. Our reaction optimization projects in the last decade focused on increasing atom efficiency and reducing energy loads. By switching to higher throughput continuous synthesis where possible, we cut overall waste and lowered incident emissions according to data collected by our environmental audits. Waste streams containing dilute chlorinated organics, which regulators monitor carefully, now undergo advanced on-site treatment to control downstream risks. Success here did not happen overnight—it took meaningful investment in process control and years of incremental upgrades to achieve these reductions. Modern batch records capture real-time energy inputs and solvent usage for every campaign, creating a benchmark for ongoing improvement. No end-user should have to choose between reliable synthetic building blocks and sustainable supplies. Our commitment bridges that divide, bringing chemical manufacturing closer to tomorrow’s environmental expectations.

    Innovation and Forward-Looking Potential

    Each year, discovery teams propose new medicinal chemistry projects using our 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine as their starting point. Despite the molecule being a staple for some, it continues to surprise those pushing beyond established boundaries. In recent years, several large-scale fluorescent probe syntheses turned to this starting material to introduce backbone rigidity and functional handles. One industrial team found success in catalyzing regioselective metalation followed by site-specific labeling—possible through judicious control over the ring’s properties bestowed by this substitution pattern. The relatively underexploited combination of chloromethyl, methoxy, and dimethyl substitution continues to show potential in specialty catalyst anchors, photoactive dye synthesis, and new crop-protection molecule candidates. Many clients ask for custom analogs developed off this core structure. Based on our direct synthetic experience, we see continued opportunity for tailored derivative building blocks further refined for unique downstream uses in the next decade.

    Supporting Knowledge and Technical Growth

    We view our role as more than just suppliers. Countless technical exchanges with university research groups and industrial labs keep us at the cutting edge of synthetic methods involving this compound. Sharing synthetic tricks, troubleshooting obscure chromatography issues, and supporting scale-up have become part of daily technical exchanges. Our staff regularly publish and review recent literature, resulting in refined batch processes and improved reactivity profiles. We regularly share best practices for loading, dispensing, and handling—especially with academic and biotech innovators who may lack in-house operational support. Multiple clients have cited us in patents and technical communications, a reflection of their confidence in our reliability and knowledge. We keep open doors to collaborative opportunities and support educational outreach programs, because the best chemistry comes from a foundation of shared knowledge and practical support at every production stage.

    Conclusion: The Value of Direct Manufacturer Expertise

    Every kilogram of 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine produced in our facility carries with it a commitment to reliability, technical excellence, and hands-on chemical expertise. The advantage comes from producing it ourselves: tighter control, direct support, and solutions drawn from real-world experience. This ensures regulatory responsibilities are met, production scaling is optimal, process risks are minimized, and project goals are met with confidence. direct access to the source allows users to focus more on innovation and less on supply-chain uncertainties. With each batch that leaves our plant, we reinforce relationships built on transparency, partnership, and shared pursuit of scientific and industrial advancement. We invite you to experience firsthand the difference that dedicated manufacturing, continuous process refinement, and real chemical knowledge can make to your ambitious projects.